RN7SL269P
pseudogene in the species Homo sapiens
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RN7SL269P
Summary
RN7SL269P is a pseudogene[1].
Key Facts
- RN7SL269P's instance of is recorded as pseudogene[2].
- RN7SL269P's instance of is recorded as gene[3].
- RN7SL269P is a type of pseudogene[4].
- RN7SL269P's genomic start is recorded as 169957942[5].
- RN7SL269P's genomic end is recorded as 169958246[6].
- RN7SL269P's found in taxon is recorded as Homo sapiens[7].
- RN7SL269P's chromosome is recorded as human chromosome 1[8].
- RN7SL269P's strand orientation is recorded as reverse strand[9].
- RN7SL269P's exact match is recorded as http://identifiers.org/ncbigene/106479320[10].
- RN7SL269P's cytogenetic location is recorded as 1q24.2[11].
- RN7SL269P's expressed in is recorded as testicle[12].
- RN7SL269P's expressed in is recorded as gonad[13].
- RN7SL269P's expressed in is recorded as epithelium of colon[14].
- RN7SL269P's expressed in is recorded as skeletal muscle tissue[15].
- RN7SL269P's expressed in is recorded as primary visual cortex[16].
- RN7SL269P's expressed in is recorded as monocyte[17].
- RN7SL269P's expressed in is recorded as prefrontal cortex[18].
- RN7SL269P's expressed in is recorded as urinary bladder[19].
- RN7SL269P's expressed in is recorded as superior frontal gyrus[20].
- RN7SL269P's expressed in is recorded as blood[21].